Literature DB >> 31811710

Baseline characteristics and long-term outcomes of eosinophilic fasciitis in 89 patients seen at a single center over 20 years.

Robert L Mango1, Kubra Bugdayli2, Cynthia S Crowson3,4, Lisa A Drage5, David A Wetter5, Julia S Lehman5,6, Margot S Peters5,6, Mark D Davis5, Vaidehi R Chowdhary7.   

Abstract

AIM: Eosinophilic fasciitis (EF) is a rare, fibrosing disorder of skin and subcutaneous tissue. This study was undertaken to describe its clinical and laboratory features and identify prognostic factors associated with outcome.
METHODS: We conducted a retrospective review of all EF patients evaluated at our institution from 1 January1997 to 30 December 2016. Kaplan-Meier methods were used to determine treatment response rates over time. Potential associations between baseline characteristics and complete response were examined using Cox models adjusted for age and sex. Time-dependent covariates were used to examine treatment effects.
RESULTS: We identified 89 EF patients, with a female-to-male ratio of 1:1. Clinical features included groove sign in 26 (29%), peau d'orange/dimpling in 22 (25%), inflammatory arthritis in 9 (10%) and muscle weakness in 9 (10%). Aldolase was elevated in 11/36 (31%). Complete response rate was 60% (95% confidence interval [CI]: 35-75) at 3 years. Diagnostic delay was inversely associated with treatment response (hazards ratio: 0.84 per 1 month increase; 95% CI: 0.73-0.98). No baseline characteristics correlated with treatment response, but a trend toward positive association of elevated aldolase, hypergammaglobulinemia and presence of hematologic disorders was noted. Methotrexate was the most commonly used immunosuppressant in 79%, hydroxychloroquine in 45%, mycophenolate mofetil in 18% and azathioprine in 8%. No single immunosuppressant agent was associated with a superior response during treatment.
CONCLUSIONS: EF is characterized by relatively high response rates. Consensus diagnostic criteria, standardized management algorithms, and large prospective multi-center cohorts are needed to develop an evidence-directed approach to this challenging condition.
© 2019 Asia Pacific League of Associations for Rheumatology and John Wiley & Sons Australia, Ltd.

Entities:  

Keywords:  eosinophilia; eosinophilic fasciitis; sclerosing disorder; thickened skin

Mesh:

Substances:

Year:  2019        PMID: 31811710     DOI: 10.1111/1756-185X.13770

Source DB:  PubMed          Journal:  Int J Rheum Dis        ISSN: 1756-1841            Impact factor:   2.454


  3 in total

Review 1.  A case of eosinophilic fasciitis without skin manifestations: a case report in a patient with lupus and literature review.

Authors:  Kohei Asaoka; Yuki Watanabe; Kazuhiro Itoh; Naoko Hosono; Tomoya Hirota; Masamichi Ikawa; Tomohisa Yamaguchi; Satomi Hatta; Yoshiaki Imamura; Ichizo Nishino; Takahiro Yamauchi; Hiromichi Iwasaki
Journal:  Clin Rheumatol       Date:  2020-09-24       Impact factor: 2.980

2.  UVA-1 phototherapy as adjuvant treatment for eosinophilic fasciitis: in vitro and in vivo functional characterization.

Authors:  Linda Tognetti; Camilla Marrocco; Andrea Carraro; Edoardo Conticini; Cyril Habougit; Giancarlo Mariotti; Elisa Cinotti; Jean Luc Perrot; Pietro Rubegni
Journal:  Int J Dermatol       Date:  2021-12-08       Impact factor: 3.204

3.  Eosinophilic Fasciitis of Wrists with a Positive Prayer Sign.

Authors:  Xia Li; Zhen Tian; Fang Kong; Yi Zhao; Xiaoxia Li
Journal:  Cureus       Date:  2020-01-07
  3 in total

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